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Principal Scientist- Toxicology
AL, USA
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Principal Scientist / Study Director (Toxicology)

Build Programs. Lead Science. Influence Outcomes.


Why This Role Matters


Here,  toxicology isn’t just about executing studies—it’s about shaping how therapies reach patients safely and effectively.

This role sits at the intersection of:

  • Scientific leadership
  • Client partnership
  • Program development

You won’t just write reports—you’ll own studies, guide strategy, and influence decision-making across entire development programs.

If you’re someone who wants to move beyond execution into true scientific leadership, this is your opportunity.


What You’ll Actually Be Doing


This is a Study Director + Program Leader hybrid role.

You will:

Own and Lead Toxicology Programs

  • Serve as Study Director across GLP and non-GLP toxicology studies
  • Design studies, interpret data, and guide IND-enabling strategies
  • Oversee full lifecycle: protocol → execution → reporting → client delivery

Be the Scientific Voice for Clients

  • Act as a trusted advisor to sponsors (biotech, pharma, government)
  • Translate complex data into clear, actionable insights
  • Guide clients through study design, risk, and regulatory considerations

Drive Scientific Breadth (Not Just Depth)

  • Work across multiple species (rodent → NHP preferred)
  • Contribute to studies involving:
  • General toxicology
  • Safety pharmacology
  • PK/toxicology (especially NHP)
  • Emerging therapeutic areas (CNS, obesity, dermatology, vaccines, oncology)

Expand and Build Capabilities

  • Help shape and grow the toxicology program
  • Contribute to:
  • New model development
  • Assay validation
  • Capability expansion

Partner Across the Business

  • Collaborate with:
  • Business Development (winning work)
  • Project Management (execution)
  • Scientific teams (delivery)
  • Contribute to proposals and scopes of work

Step Into Leadership

  • Mentor junior scientists and study team members
  • Begin transitioning toward program leadership and team oversight
  • Play a key role in scaling scientific operations


What Success Looks Like


You’re not just “doing studies”—you’re:

  • Leading complex, multi-study programs
  • Becoming a go-to scientific leader internally and externally
  • Helping clients move therapies forward with confidence
  • Growing into a manager of people and programs


Who This Role Is Built For


Technically Strong, But Ready for More

You likely have:

  • 5–7+ years in toxicology (CRO experience strongly preferred)
  • Experience as a Study Director (or ready to step fully into it)
  • Strong foundation in GLP toxicology


Scientifically Broad

  • Exposure to multiple species (NHP experience is a major plus)
  • Experience across:
  • General tox
  • Safety pharmacology
  • PK/tox
  • Comfortable with complex dosing routes (e.g., intrathecal, intracranial)

Client-Facing Mindset


This is critical.

You:

  • Communicate clearly and confidently with clients
  • Think in terms of service, not ego
  • Can guide without dominating

Future Leader (Even If You’re Not One Yet)

You may not have large team management experience yet—but:

  • You want to grow into it
  • You’re ready to take ownership of larger programs
  • You think beyond your individual contribution

Preferred (But Not Required)

  • DABT (or actively pursuing)
  • NHP experience (especially PK/tox)
  • IND-enabling study experience
  • Experience across diverse therapeutic areas

Why This Role Is Different

Most “Senior Scientist” roles:

  • Focus on execution
  • Limit client interaction
  • Keep you in a narrow lane

This role:

  • Gives you ownership
  • Builds your scientific voice
  • Positions you for leadership


Career Trajectory

This role is intentionally designed as a launchpad into leadership:

  • Program leadership
  • Team management
  • Expanded scientific influence

You’re not being hired to stay in place—you’re being hired to grow into something bigger.


About the Organization

We have  been translating science into real-world solutions since 1941, supporting drug development from discovery through preclinical and beyond.

You’ll be joining a team focused on:

  • Advancing life-saving therapies
  • Delivering high-quality science
  • Building long-term client partnerships


Compensation & Benefits


  • Competitive compensation aligned with experience level
  • Full benefits package (medical, dental, vision, 401k, PTO, etc.)
  • Support for continued professional development (including DABT)


This is an onsite/ close proximity role. Take a look at what the area has to offer: Relocation Guide

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